Synthesis and Anti-tumor Activity Evaluation of Rhein-Aloe Emodin Hybrid Molecule

被引:1
作者
Yuan, Ye-fei [1 ,2 ,3 ]
Hu, Xiang-yu [2 ]
He, Ying [2 ]
Deng, Jia-gang [4 ]
机构
[1] Guangxi Med Univ, Nanning 530021, Guangxi, Peoples R China
[2] Luzhou Med Coll, Luzhou 646000, Sichuan, Peoples R China
[3] Guangxi Boise Natl Agr Sci Tech Zone, Baise 533612, Guangxi, Peoples R China
[4] Guangxi Tradit Chinese Med Univ, Nanning 530001, Guangxi, Peoples R China
关键词
Rhein; Aloe-emodin; Rhein-aloe emodin hybrid molecule; SQUAMOUS-CELL CARCINOMA; MECHANISMS; APOPTOSIS; DEATH;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
To improve the anti-tumor effects of rhein and aloe-emodin, a rhein-aloe-emodin hybrid molecule (RH-AE) was synthesized from rhein and aloe-emodin in the presence of dicyclohexylcarbodiimide (DCC) and 4-dimethylaminopyridine (DMAP). Chemical and spectroscopic methods, such as H-1 and C-13 NMR spectroscopy, and HR-ESIMS were used for the structure identification of RH-AE. Using the cell counting kit-8 (CCK-8) assay, the in vitro anti-tumor effects were compared between RH-AE, rhein and aloe-emodin on human hepatoma HepG2, human nasopharyngeal carcinoma CNE, human lung cancer NCI-H460, human ovarian cancer SK-OV-3, and human cervical cancer Hela cells. The results showed that the half inhibitory concentration (IC50) of RH-AE on HepG2, CNE, NCI-H460, SK-OV-3, and Hela cells were significantly lower than those of rhein and aloe-emodin. This showed that RH-AE has a better in vitro anti-tumor effect than rhein and aloe-emodin.
引用
收藏
页码:207 / 210
页数:4
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